Canonical Allele Identifier: CA354793932

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142168417G>C (hg19) ; chr3:g.142449575G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449575G>C , CM000665.2:g.142449575G>C	GRCh38
NC_000003.11:g.142168417G>C , CM000665.1:g.142168417G>C	GRCh37
NC_000003.10:g.143651107G>C	NCBI36
NG_008951.1:g.134252C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.7789C>G MANE Select	ENSP00000343741.4:p.Gln2597Glu
ENST00000513291.2:n.6498C>G
ENST00000653893.1:n.2647C>G
ENST00000654170.1:n.2632C>G
ENST00000656114.1:n.2875C>G
ENST00000656590.1:c.6716C>G
ENST00000658083.1:n.2969C>G
ENST00000661310.1:c.7597C>G	ENSP00000499589.1:p.Gln2533Glu
ENST00000665483.1:n.5329C>G
ENST00000666447.1:n.4292C>G
ENST00000666943.1:n.4521C>G
ENST00000350721.8:c.7789C>G	ENSP00000343741.4:p.Gln2597Glu
ENST00000504521.5:c.378C>G	ENSP00000422553.1:n.378C>G
ENST00000513291.1:c.4853C>G
ENST00000515810.1:c.215C>G	ENSP00000421870.1:n.215C>G
NM_001184.3:c.7789C>G	NP_001175.2:p.Gln2597Glu
XM_011512924.1:c.7795C>G	XP_011511226.1:p.Gln2599Glu
XM_011512925.1:c.7603C>G	XP_011511227.1:p.Gln2535Glu
XR_924147.1:n.10546C>G
XR_924148.1:n.8021C>G
NM_001354579.1:c.7597C>G	NP_001341508.1:p.Gln2533Glu
XR_001740179.2:n.8015C>G
XR_924148.2:n.8021C>G
NM_001184.4:c.7789C>G MANE Select	NP_001175.2:p.Gln2597Glu
NM_001354579.2:c.7597C>G	NP_001341508.1:p.Gln2533Glu